Method of preparing organo dialkylalkoxysilane

ABSTRACT

The invention relates to the preparation of organodialkylalkoxysilane using a continuous method consisting in bringing an alkanol into continuous contact with an omega-haloalkyl dialkylhalosilane in a countercurrent reactor, such as a plate column or a packed column. The reaction is performed in the aforementioned countercurrent reactor in the presence or absence of a non-reactive solvent with scavenging of the hydrochloric acid formed. The omega-haloalkyl dialkylalkoxysilane thus formed is particularly suitable for use as a starting material for the preparation of organosilicon compounds containing sulphur having general formula (I) by means of sulphidisation reaction on an alkaline metal polysulphide.

CROSS-REFERENCE TO PRIORITY/PCT APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 11/499,585, filed Aug. 4, 2006, now abandoned which is a divisional of U.S. patent application Ser. No. 10/518,685, filed Jun. 23, 2005, and claims priority under 35 U.S.C. § 119 of FR 02/07713, filed Jun. 21, 2002 and FR 02/15114, filed Dec. 2, 2002, each hereby expressly incorporated by reference in its entirety and each assigned to the assignee hereof.

The present invention relates to a process for preparing organo dialkylalkoxysilane by a continuous process in the presence of an alkanol on an omega-haloalkyl dialkylhalosilane.

The invention relates more particularly to the preparation of an ethoxypropylsilane from a chloropropylsilane. Known processes on this synthesis relate more specifically to dichloropropylsilane and trichloropropylsilane. The process according to the invention allows 3-chloropropyldimethylchlorosilane to be used as reactant, while giving ethoxydimethy1-3-chloropropylsilane with very high yields. The chemical reaction is as follows: ClMe₂Si—CH₂CH₂CH₂Cl+EtOH→(EtO)Me₂Si—CH₂CH₂CH₂Cl+HCl

The 3-chloropropyldimethylchlorosilane may be ethoxylated quantitatively and selectively in the presence of a base. The use, for example, of an organic base of tertiary amine type (including triethylamine) allows the acid formed to be neutralized stoichiometrically. However, the use of a base, and the lengthening and complication of the process that are associated with its use and its eventual removal, constitute a certain disadvantage. In the absence of base, moreover, the reaction leads to performance levels which are unsatisfactory under conditions conventionally used for this type of reaction: running ethanol into an initial charge of 3-chloropropyldimethylchlorosilane. This is a batch reactor process which gives excellent results only if the raw material is dichloropropylmethylchlorosilane or trichloropropylchlorosilane: degree of conversion (DC)=100% and selectivity (RT)>95%. This is because the specificity of the dimethylchlorosilane moiety, compared for example with the trichlorosilane group, leads to a lower reactivity with respect to ethanol and, consequently, gives rise to more substantial formation of secondary products. These secondary products have come essentially from an oligomerization of the silane function, a reaction consecutive to the following reaction: EtOH+HCl→EtCl+H₂O 2[ClMe₂Si—CH₂CH₂CH₂Cl]+H₂O→ClCH₂CH₂CH₂—SiMe₂-O-Me₂Si—CH₂CH₂CH₂Cl+HCl

The principal aim of the present invention is specifically to provide a high-performance process, of the type above, whose starting product is a monochlorotriorganosilane, especially 3-chloropropyldimethylchlorosilane, and which can be carried out in the absence of base.

This aim, among others, is achieved by the present invention, which relates in effect to a process for preparing organodialkylalkoxysilane by a continuous process which consists in contacting an alcohol, of alkanol type for example, continuously in countercurrent with an omega-haloalkyldialkylhalosilane.

The conversions obtained are generally greater than 90% and may reach 100%, and the selectivities obtained are also very high.

The alcoholysis reaction deployed according to the invention may be represented schematically by the following equation:

where:

-   -   the symbol Hal represents a halogen atom selected from chlorine,         bromine and iodine atoms, the chlorine atom being preferred,     -   the symbols R¹, which are identical or different, each represent         a monovalent hydrocarbon group selected from a linear or         branched alkyl radical having 1 to 15 carbon atoms and a linear         or branched alkoxyalkyl radical having 2 to 8 carbon atoms;     -   the symbols R² and R³, which are identical or different, each         represent a monovalent hydrocarbon group selected from a linear         or branched alkyl radical having 1 to 6 carbon atoms and a         phenyl radical;     -   A represents a removable group selected alternatively from: a         halogen atom Hal belonging to chlorine, bromine and iodine         atoms, the chlorine atom being preferred; or a radical         para-R⁰—C₆H₄—SO₂-0- where R⁰ is a linear or branched C1-C4 alkyl         radical, the tosylate radical para-CH₃—C₆H₄—SO₂—O— being         preferred; or a radical R⁰—SO₂-0- where R⁰ is as defined above,         the mesylate radical CH₃—SO₂-0- being preferred; or a radical         R⁰—CO—O— where R⁰ is as defined above, the acetate radical         CH₃—CO—O— being preferred, the most preferred radical A being         the chlorine atom.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic of an exemplary embodiment of a reaction apparatus.

According to the invention the continuous process therefore makes it possible to carry out, in a countercurrent reactor, both the alkoxylation reaction and the separation of the stream of alkanol of formula (VIII) and of H-Hal (generally HCl) from the stream of silanes. Subsequently it is possible, if desired, finally to separate the alkanol from the H-Hal. Thereafter the alcohol thus purified can be reinjected into the reactor.

More specifically the procedure is such that within the reactor a descending liquid fluid comprising the silane of formula (VII) and an ascending gaseous fluid comprising the alcohol of formula (VIII) will circulate in countercurrent. Also present within the reactor, in the vapor state, is the product of formula H-Hal. Advantageously the inside of the reactor in which the alcoholysis reaction is carried out is composed of a packed column or a plate column so as to create reaction zones in liquid phase: the temperature is between the boiling temperature of the alcohol of formula (VIII) and the boiling temperature of the silane of formula (VII). The reaction is carried out in the reactor alternatively at atmospheric pressure or at reduced pressure or at superatmospheric pressure.

In the advantageous implementation of the invention the alcohol is introduced into the boiler and/or into the lower part of the column. The silane, for its part, is introduced at a location anywhere on the column above the zone where the alcohol is introduced. In this case the silane descends the column in countercurrent and reacts in countercurrent with the vaporized ethanol, which carries the HCl formed to a condenser situated at the top of the column, or else the mixture in the vapor state is separated elsewhere. The alkoxylated silane is recovered at the bottom of the column, in the boiler, and/or is taken off at the side in the lower part of the column.

The process comprises the stripping or vapor entrainment of the HCl formed from the reaction mixture and the shifting of the equilibrium by increasing the concentration of alkanol (ethanol) by distilling ethanol from the reaction mixture in order to remove HCl.

It is preferable, so as always to have an excess of alcohol, to operate the reactor by working with an alcohol/silane molar ratio of greater than 1 and, preferably, between 1.2 and 20. In the case of the ethanol/3-chloropropyldimethylchlorosilane pairing, this alcohol/silane molar ratio is greater than 1.2 and preferably greater than 3, and generally is at most 20. It is preferable, moreover, in the advantageous implementation of the invention, to introduce the alcohol in the lower part of the column and the silane in the upper part of the column.

The column may be equipped in its internal structure with dumped or ordered packing or else with plates. Controlling the reflux rate is an advantageous means for adjusting the profile of temperatures in the column, but particularly for regulating the amount of H-Hal present in the column.

One operational improvement of this countercurrent reactor may consist in at least one side removal of the gaseous streams based on alcohol and on H-Hal at one or more locations of the column, in order to minimize the concentration of Hal in the reactor. It is known that H-Hal which is not removed can limit the shifting of the reaction at equilibrium and may give rise to parasitic reactions. A fresh alcohol stream or a stream resulting from recycling of the acidic alcohol may be injected into each removal zone in order to compensate the fluid removed.

As indicated above, in the case where the products corresponding to formulae (VII), (VIII) and (IX) have ethyl groups R¹ and methyl groups R² and R³ and A and Hal represent a chlorine atom, the alcohol is an alcohol constituted by ethanol and the silane is 3-chloropropyldimethylchlorosilane, with formation of HCl.

If the reaction is conducted at atmospheric pressure the reaction temperature within the reactor, and in particular within the column, must be greater than that of the stripping carrier gas, i.e., for example, 78° C. in the case of ethanol, and less than the temperature of the 3-chloropropyldimethylchlorosilane, i.e., 178° C. It is therefore recommended to operate at reduced pressure in order to limit the solubility of HCl in the ethanol and to conduct the reaction at a temperature less than that corresponding to one atmospheric pressure, which allows the parasitic reactions to be limited and selectivity gains to be made.

The acidic alcohol, in other words the alcohol laden with HCl, must be purified before being recycled into the reaction mixture, by distillation, azeotropic distillation where appropriate, by adsorption on resin, by neutralization or by membrane separation.

The stripping of the HCl may be coupled with a stripping of the water present in the mixture, by operating at a temperature greater than the boiling temperature of water at the pressure in question.

The alcoholysis reaction in this countercurrent reactor may be carried out optionally in the presence of an organic solvent and/or an inert gas. The solvent is aprotic and relatively nonpolar, such as aliphatic and/or aromatic hydrocarbons. The solvent used has a boiling temperature at the service pressure (atmospheric pressure) of between the boiling temperature of the alcohol of formula (VIII), for example 77.8° C. for ethanol, and that of the silane of formula (VII), for example 178° C. for 3-chloropropyldimethylchlorosilane. As an appropriate solvent for the ethanol/3-chloropropyldimethylchlorosilane pairing mention may be made in particular of toluene, monochlorobenzene and xylene. The function of the solvent is to strip the hydrochloric acid (HCl) by mechanical entrainment (the alcohol is also entrained, and recycling after purification may be contemplated) and also to create a depletion zone (no HCl, or very little, at the bottom of the column) in order to minimize the parasitic chemical reactions.

The organodialkylalkoxysilane of formula (IX) thus obtained can be used more particularly as a starting product for preparing organosilicon compounds containing sulfur, of the general average formula (I):

in which:

x is an integral or fractional number ranging from 1.5±0.1 to 5±0.1; and the symbols R¹, R², R³, Hal and A are as defined above.

In the formula (I) above, the preferred radicals R¹ are selected from the following radicals: methyl, ethyl, n-propyl, isopropyl, n-butyl, CH₃OCH₂—, CH₃OCH₂CH₂— and CH₃OCH(CH₃)CH₂—; more preferably the radicals R¹ are selected from the following radicals: methyl, ethyl, n-propyl and isopropyl.

The preferred radicals R² and R³ are selected from the following radicals: methyl, ethyl, n-propyl, isopropyl, n-butyl, n-hexyl and phenyl; more preferably the radicals R² and R³ are methyls.

The integral or fractional number x ranges preferably from 3±0.1 to 5±0.1 and more preferably from 3.5±0.1 to 4.5±0.1.

The polysulfur monoorganoxysilanes corresponding to the formula (I) which are a specific objective of the present invention are those of formula:

in which the symbol x is an integral or fractional number ranging from 1.5±0.1 to 5±0.1, preferably from 3±0.1 to 5±0.1 and more preferably from 3.5+0.1 to 4.5±0.1.

In the present specification it will be specified that the symbol x in the formulae (I), (II), (III) and (IV) is an integral fractional number representing the number of sulfur atoms present in one molecule of formula (I), (II), (III) and (IV).

In practice this number is the average of the number of sulfur atoms per molecule of compound under consideration, insofar as the selected synthesis route gives rise to a mixture of polysulfur products each having a different number of sulfur atoms. The polysulfur monoorganoxysilanes synthesized are in fact composed of a distribution of polysulfides, ranging from the monosulfide to heavier polysulfides (such as S_(≧5), for example) centered on an average molar value (value of the symbol x) which is situated within the general ranges (x ranging from 1.5±0.1 to 5±0.1), preferentially (x ranging from 3±0.1 to 5±0.1) and more preferentially (x ranging from 3.5±0.1 to 4.5±0.1) mentioned above.

The products of formula (I) may be prepared as follows from the organodialkylalkoxysilane of formula (IX) prepared beforehand in the course of step b) by the continuous process of the invention, by reacting said product of formula (IX) in the course of step c) with an alkali metal polysulfide of formula (X) in accordance with the following reaction scheme:

step c):

where:

-   -   the symbols R¹, R², R³, A and x are as defined above,     -   the symbol M represents an alkali metal,     -   the reaction is carried out:         -   by reacting, at a temperature ranging from 20° C. to 120°             C., either the reaction mixture obtained at the end of step             (b), or the monoorganoxydiorganosilyl propyl derivative of             formula (IX), taken in isolation after separation from said             reaction mixture, with the metal polysulfide of formula (X)             in the anhydrous state, using 0.5±15 mol % of metal             polysulfide of formula (X) per mole of the reactant of             formula (IX) and optionally operating in the presence of an             inert polar (or nonpolar) organic solvent,         -   and by isolating the bis(monoorganoxysilylpropyl)             polysulfide of formula (I) that is formed.

The continuous process according to the present invention allows access to bis(monoorganoxysilylpropyl) polysulfides of formula (I). The diorganohalosilanes of formula (VII) can be prepared advantageously on the industrial scale by a process such as, in particular, that described in WO-A-99/31111, cited as reference.

The process according to the invention for preparing products of formula (I) proceeds virtually quantitatively, without employing reactants and/or without forming secondary products which are toxic compounds or pollutants to the environment (such as H₂S and alkali metals in the case of the polysulfiding step).

The starting product in step b) of formula (VII) can be prepared according to the following process:

Step a)

where:

-   -   the symbol Hal represents a halogen atom selected from chlorine,         bromine and iodine atoms, the chlorine atom being preferred, and     -   the symbols A, R² and R³ are as defined above, the reaction         being carried out:         -   by reacting, at a temperature ranging from −10° C. to 200°             C., one mole of the diorganohalosilane of formula (V) with a             molar amount which is stoichiometric or different from the             stoichiometry of the allyl derivative of formula (VI), the             operation being carried out in a homogeneous or             heterogeneous medium in the presence of an initiator             consisting:         -   either of a catalytic activator consisting of: (i) at least             one catalyst comprising at least one transition metal or one             derivative of said metal, taken from the group consisting of             Co, Ru, Rh, Pd, Ir and Pt; and optionally (2i) at least one             hydrosilylation reaction promoter,         -   or of a photochemical activator, consisting in particular of             appropriate ultraviolet radiation or appropriate ionizing             radiation, and optionally by isolating the             diorganohalosilylpropyl derivative of formula (VII) that is             formed.

According to one particularly suitable embodiment of the invention the process which has just been described consists in linking together steps (a), (b) and (c) in the definition of which the products of formulae (I), (V), (VI), (VII), (VIII) and (IX) have ethyl groups R¹ and methyl groups R² and R³ and the removable group A corresponds to the symbol Hal representing a halogen atom selected from chlorine, bromine and iodine atoms, and, preferably, a chlorine atom.

Step (a) consists in reacting the diorganohalosilane of formula (V) with the allyl derivative of formula (VI) in the presence of a selected initiator. The initiator used embraces all of the initiators, corresponding to the types indicated above, which are effective in activating the reaction between a ≡SiH function and an ethylenic unsaturation.

According to one preferred arrangement concerning the initiator, the latter is selected from catalytic activators. These catalytic activators comprise:

-   -   as the catalyst (or catalysts), (i): (i-1) at least one finely         divided elemental transition metal; and/or (i-2) a colloid of at         least one transition metal; and/or (i-3) an oxide of at least         one transition metal; and/or (i-4) a salt transition metal         and/or (i-5) a complex equipped with organic or more heteroatoms         and/or (i-6) a salt as derived from at least one a mineral or         carboxylic acid; of at least one transition metal ligand(s)         which may possess one and/or organosilicon ligands; defined         above in which the metal moiety is equipped with ligand(s) as         also defined above; and/or (i-7) a metal species selected from         the aforementioned species (elemental transition metal, oxide,         salt, complex, complexed salt) where the transition metal is         combined this time with at least one other metal selected from         the class of the elements of groups 1b, 2b, 3a, 3b, 4a, 4b, 5a,         5b, 6b, 7b and 8 (with the exception of Co, Ru, Rh, Pd, Ir and         Pt) of the Periodic Table as published in “Chemistry and         Physics, 65^(th) edition, 1984-1985, CRC Press, Inc.”, said         other metal being taken in its elemental form or in a molecular         form, it being possible for said combination to give rise to a         bimetallic or polymetallic species; and/or (1-8) a metal species         selected from the aforementioned species (elemental transition         metal and transition metal/other metal combination; oxide, salt,         complex and complexed salt on a transition metal base or on a         transition metal/other metal combination base which is supported         on an inert solid support such as alumina, silica, carbon black,         a clay, titanium oxide, an aluminosilicate, a mixture of         aluminum and zirconium oxides, or a polymer resin;     -   as the optional promoter (or promoters) (2i): a compound, which         may take for example the form of a ligand or of an ionic         compound, taken in particular from the group consisting of: an         organic peroxide; a carboxylic acid; a carboxylic salt; a         tertiary phosphine; an amine; an amide; a linear or cyclic         ketone; a trialkylhydrosilane; benzothiazole; phenothiazine; a         trivalent metal —(C₆H₅)₃ compound where metal=As, Sb or P; a         mixture of amine or of cyclohexanone with an organosilicon         compound containing one or more ≡Si—H groups; the compounds         CH₂═CH—CH₂—OH or CH₂═CH—CH₂—OCOCH₃; a lactone; a mixture of         cyclohexanone with triphenylphosphine; an ionic compound such as         for example a nitrate or a borate of an alkali metal or of         imidazolinium, a phosphonium halide, a quaternary ammonium         halide or a tin(II) halide.

According to one more preferred arrangement concerning the initiator, the latter is selected from the preferred catalytic activators mentioned above which comprise, as the catalyst (or catalysts) (i), one and/or other of the metallic species (i-1) to (i-8) where the transition metal belongs to the following subgroup: Ir and Pt.

According to one even more preferred arrangement concerning the initiator, the latter is selected from the preferred catalytic activators mentioned above which comprise, as the catalyst (or catalysts) (i), one and/or other of the metallic species (i-1) to (i-8) where the transition metal is Ir. In the context of this even more preferred arrangement, suitable Ir-based catalysts are especially:

-   -   [IrCl(CO)(PPh₃)₂]     -   [Ir(CO)H(PPh₃)₃]     -   [Ir(C₈H₁₂)(C₅H₅N)P(C₆H₁₁)3]PF₆     -   [IrCl₃], nH₂O     -   H₂[IrCl₆], nH₂O     -   (NH₄)₂IrCl₆     -   Na₂IrCl₆     -   K₂IrCl₆     -   Klr(NO)Cl₅     -   [Ir(C₈H₁₂)₂]⁺BF₄ ⁻     -   [IrCl(CO)₃]n     -   H₂IrCl₆     -   Ir4(CO)₁₂     -   Ir(CO)₂(CH₃COCHCOCH₃)     -   Ir(CH₃COCHCOCH₃)     -   IrBr₃     -   IrCl₃     -   IrCl₄     -   IrO₂     -   (C₆H₇)(C₈H₁₂)Ir.

In the context of the even more preferred arrangement mentioned above, other Ir-based catalysts which are even more suitable are taken from the group of the iridium complexes of formula: [Ir(R⁴)Hal]₂  (XI) where:

-   -   the symbol R⁴ represents a conjugated or nonconjugated, linear         or cyclic (mono- or polycyclic) polyene ligand having 4 to 22         carbon atoms and from 2 to 4 ethylenic double bonds;     -   the symbol Hal is as defined above.

As an example of iridium complexes of formula (XII) which are even more suitable mention will be made of those in whose formula:

-   -   -   the symbol R⁴ is selected from 1,3-butadiene, 1,3-hexadiene,             1,3-cyclohexadiene, 1,3-cyclooctadiene, 1,5-cyclooctadiene,             1,5,9-cyclododecatriene and norbornadiene and         -   the symbol Hal represents a chlorine atom.

As specific examples of iridium complexes which are even more suitable mention will be made of the following catalysts:

-   -   di-μ-chlorobis(η-1,5-hexadiene)diiridium,     -   di-μ-bromobis(η-1,5-hexadiene)diiridium,     -   di-μ-iodobis(η-1,5-hexadiene)diiridium,     -   di-μ-chlorobis(η-1,5-cyclooctadiene)diiridium,     -   di-μ-bromobis(η-1,5-cyclooctadiene)diiridium,     -   di-μ-iodobis(η-1,5-cyclooctadiene)diiridium,     -   di-μ-chlorobis(η-2,5-norbornadiene)diiridium,     -   di-μ-bromobis(η-2,5-norbornadiene)diiridium,     -   di-μ-iodobis(η-2,5-norbornadiene)diiridium.

The catalyst may be used—and this is another preferential arrangement—in a homogeneous medium, as described in JP-B-2 938 731. In this context the reaction may be conducted continuously, semicontinuously or batchwise. At the end of operation the product of the reaction is separated and collected by distillation of the reaction mixture, and the catalyst can be recycled by producing a new charge of reactants on a distillation residue containing the catalyst from the distillation step of the product of the preceding operation, with complementary addition of new catalyst where appropriate. Where complexes are employed the recycling of the catalyst can be enhanced by further adding a small amount of ligand.

The catalyst may also be used in heterogeneous medium. This operating method has recourse in particular to the employment of a catalyst which is supported on an inert solid support of the type of those defined above. This operating method makes it possible to carry out the reaction in a fixed-bed reactor operating continuously, semicontinuously or batchwise with recycling. It is also possible to carry out the reaction in a standard stirred reactor operating continuously, semicontinuously or batchwise.

As far as the other reaction conditions are concerned, the reaction is carried out within a wide range of temperatures, ranging preferably from −10° C. to 100° C., under atmospheric pressure or under a pressure greater than atmospheric pressure, which may reach or even exceed 20×10⁵ Pa.

The amount of the allyl derivative of formula (VI) used is preferably from 1 to 2 mol per mole of organosilicon compound. As for the amount of catalyst(s) (i), expressed by weight of transition metal taken from the group consisting of Co, Ru, Rh, Pd, Ir and Pt, it is situated within the interval ranging from 1 to 10 000 ppm, preferably ranging from 10 to 2000 ppm and more preferably ranging from 50 to 1000 ppm, these figures being based on the weight of organosilicon compound of formula (V) or (IX). The amount of promoter(s) (2i), when one or more promoters are used, expressed in numbers of moles of promoter(s) per gram-atom of transition metal taken from the group consisting of Co, Ru, Rh, Pd, Ir and Pt, is situated in the interval ranging from 0.1 to 1000, preferably ranging from 0.5 to 500 and more preferably ranging from 1 to 300. The diorganohalosilylpropyl derivative of formula (VII) is obtained with a molar yield of at least 80%, based on the starting organosilicon compound of formula (V).

According to one preferred arrangement the anhydrous metal polysulfides of formula (X) are prepared by reacting an alkali metal sulfide, optionally containing water of crystallization, of formula M₂S (XII), in which the symbol M has the meaning given above (alkali metal), with elemental sulfur, operating at a temperature ranging from 60° C. to 300° C., optionally under pressure and also optionally in the presence of an anhydrous organic solvent.

Advantageously the alkali metal sulfide M₂S employed is the industrially available compound, which is generally in the form of a sulfide hydrate: one alkali metal sulfide of this type which is highly suitable is the Na₂S sulfide available commercially, which is a hydrated sulfide containing 55 to 65% by weight of Na₂S.

According to a more preferred arrangement for conducting step (c) the anhydrous metal polysulfides of formula (X) are prepared beforehand from an alkali metal sulfide M₂S in the form of a hydrated sulfide, according to a procedure which consists in linking together the following operating phases (1) and (2):

-   -   phase (1), where the alkali metal sulfide hydrate is dehydrated         by applying the appropriate method which makes it possible to         remove the water of crystallization while retaining the alkali         metal sulfide in the solid state throughout the dehydration         phase;     -   phase (2), where subsequently one mole of dehydrated alkali         metal sulfide obtained is contacted with n(x−1) moles of         elemental sulfur, the operation being carried out at a         temperature ranging from 20° C. to 120° C., optionally under         pressure and optionally again in the presence of an anhydrous         organic solvent, the aforementioned factor n being situated         within the range from 0.8 to 1.2 and the symbol x being as         defined above.

With regard to phase (1), as a highly suitable dehydration protocol mention will be made in particular of the drying of the hydrated alkali metal sulfide, operating under a partial vacuum ranging from 1.33×10² Pa to 40×10² Pa and bringing the compound to be dried to a temperature ranging, at the beginning of drying, from 70° C. to 85° C., then by gradually raising the temperature in the course of drying from the zone ranging from 70° C. to 85° C. until it reaches the zone ranging from 125° C. to 135° C., in accordance with a program which envisages a first temperature rise of +10° C. to +15° C. after a first period varying from 1 hour to 6 hours, followed by a second temperature rise of +20° C. to +50° C. after a second period varying from 1 hour to 4 hours.

With regard to phase (2), as a highly suitable sulfiding protocol mention will be made of the implementation of this reaction in the presence of an anhydrous organic solvent; appropriate solvents are, in particular, lower (C1-C4) aliphatic alcohols which are anhydrous, such as anhydrous methanol or ethanol, for example. The number of atoms of elemental sulfur S_(x) in the metal polysulfide M₂S_(x) is a function of the molar ratio of S with respect to M₂S; for example, the use of 3 mol of S (n=1 and x−1=3) per mole of M₂S gives the alkali metal tetrasulfide of formula (X) where x=4.

To return from this to the implementation of step (c), this latter step is carried out in a wide range of temperatures, ranging preferably from 50° C. to 90° C., operating more preferably in the presence of an organic solvent and, in that context, making use advantageously of the alcohols referred to above with regard to the conduct of phase (2).

The product M-A, and in particular the halide M-Hal, formed in the course of reaction is generally removed at the end of the step by means for example of filtration.

The bis(monoorganoxydiorganosilylpropyl) polysulfide of formula (I) that is formed is obtained with a molar yield of at least 80%, based on the starting monoorganoxydiorganosilylpropyl derivative of formula (IX).

The examples which follow illustrate the present invention without limiting its scope; reference will be made to the attached drawing, in which the single FIGURE represents diagrammatically the reaction apparatus including a column which is used in said examples.

In the single FIGURE it can be seen that the apparatus 1 comprises at its base a boiler 2 and a column 3 with a diameter of 40 mm, comprising a lower part 4 including the foot of the column and an upper part 5 including the head of the column. The column contains 15 plates labeled 1 to 15. The plates are made of perforated glass. The column 3 is equipped with an ethanol feed tank 6, which feeds the boiler 2 and certain plates of the bottom part 4 of the column, and also with a liquid recovery tank 7. The column 3 is equipped with a second feed tank 8 for optional feeding with liquid ethanol, which allows some of the plates in the upper part 5 of the column 3 to be fed, in order to simulate a purified ethanol reflux. The column 3 has an ethanol recovery tank 9 which constitutes the distillate and a starting silane feed tank 10. The silane is introduced onto a plate in the upper part 5 of the column, and the ethanol in the lower part. The upper part 5 of the column is surmounted by a condenser 11 connected via the pipeline 12 to the HCl suppression column 13 (HCl trap).

EXAMPLE 1

This example describes the preparation of bis(monoethoxydimethylsilylpropyl) tetrasulfide of formula (III) in which the number x is centered on 4.

The reaction scheme concerned by this example is the following one:

Step (a):

Step (b):

Step (c):

in which the reactant 6 is obtained according to the following equation:

1) Step (a): Synthesis of 3:

A 1 liter stirred glass reactor equipped with a jacket and a stirrer and surmounted by a distillation column is charged with 165 g of allyl chloride 2 with a purity of 97.5% by weight (2.10 mol) and 0.229 g of catalyst [Ir(COD)Cl]₂ where COD=1,5-cyclooctadiene and the mixture is stirred in order to dissolve the catalyst completely. The temperature of the mixture is adjusted to 20° C. using the heat-exchange fluid circulating in the jacket.

Dimethylhydrochlorosilane 1, with a purity of 99% by weight, is introduced into the reaction mixture via a dip tube, using a pump: 196.5 g (2.06 mol) of 1 are introduced over 2 hours 35 minutes. The flow rate of introduction is adjusted in order to maintain the temperature of the reaction mixture at between 20 and 25° C., taking into account the strongly exothermic nature of the reaction. The reaction mixture is kept with stirring for 20 minutes after the end of the introduction of the dimethylhydrochlorosilane 1.

At the end of the stirring time a sample is taken for analysis. The results are as follows: degree of conversion of the dimethylhydrochlorosilane 1=99.8%, and selectivity for chloropropyldimethylchlorosilane 3=92.7% (by analysis by gas chromatography).

The reaction mixture is subsequently distilled under vacuum (approximately 35×10² Pa) at approximately 40° C. to give two main fractions: ∈ the light products (residual allyl chloride 2 and residual traces of dimethylhydrochlorosilane 1, accompanied essentially by chloropropyldimethylchlorosilane 3; ∉ chloropropyldimethylchlorosilane 3, with a molar purity of more than 98%. A distillation residue consisting of heavier products, and catalyst, then remains. Molar yield: 85%.

2) Step (b): Synthesis of 5:

As indicated above, a column as shown in the single FIGURE is used. Chloropropyldimethylchlorosilane, stored in the feed tank 10, and ethanol, stored in the feed tanks 1 and 3, are injected directly into column 1, at plates 13 and 3 respectively. The column 1 is charged with an appropriate inert solvent, in the present case toluene. The function of the solvent is to strip the hydrochloric acid (HCl) by mechanical entrainment, the ethanol also being entrained and optionally recycled after purification. The solvent also creates a depletion zone (no HCl or very little in the lower part of the column), thereby making it possible to restrict the incidence of parasitic chemical reactions.

Toluene is brought to boiling in the boiler (2) by means of electrical resistors. This startup phase takes place with total reflux of the column in order to charge the plates of the column. Thereafter the reflux rate is regulated by a valve situated between the condenser (6) and the distillate recovery tank (4) but not shown in the single FIGURE.

The ethanol is injected into the column in liquid or vapor phase at plate 3 of the lower part 4 of the column. The ethanol flow rate is 100 g/h. The chloropropyldimethylchlorosilane is injected at plate 13 in liquid phase, with a flow rate of 120 g/h. The EtOH: silane molar ratio is 3.17.

The ethanol vaporizes in the column and, during its ascension, meets the chloropropyldimethylchlorosilane in liquid phase which is descending toward the boiler. The experiment lasts for 5 hours and the overall degree of conversion of chloropropyldimethylchlorosilane to chloropropyldimethylethoxysilane is from 92% to 94% with a selectivity of more than 90%.

3) Step (c): Synthesis of 7:

3.1) Preparation of Anhydrous Na₂S₄ 6:

-   -   Phase 1: Drying of Na₂S Hydrate:

43.6 g of industrial Na₂S hydrate flakes containing approximately 60.5% by weight of Na₂S are introduced into the 1-liter round-bottomed glass flask of a rotary evaporator. The flask is placed under an argon atmosphere and then under reduced pressure at 13.3×10² Pa.

The flask is immersed in an oil bath, whose temperature is then brought to 76° C. This temperature is maintained for 2 hours. Subsequently a protocol for increasing the temperature of the oil bath is applied in order to avoid melting the Na₂S, which occurs between 85 and 90° C. approximately. The purpose of the gradual increase in temperature is to accompany the change in the melting temperature of the product to be dried, which increases when the product undergoes dehydration. The protocol applied is as follows: 1 hour at 82° C., 2 hours at 85° C., 1 hour at 95° C., 1 hour at 115° C. and finally 1 hour at 130° C. It should be noted that this protocol can be modified according to the amount to be dried, the operating pressure and other parameters effecting the rate at which the water is removed. The amount of water removed, measured by mass difference, is 17.2 g, corresponding to a moisture content of 39.5% by weight.

-   -   Phase 2: Synthesis of Na₂S₄ 6:

The Na₂S (26 g) dried according to the protocol described above is placed in suspension in 400 ml of anhydrous ethanol and transferred by suction into a stirred, jacketed, one-liter glass reactor equipped with a condenser with a possibility for reflux. 31.9 g of sulfur and also 200 ml of anhydrous ethanol are additionally introduced into this reactor. The temperature of the mixture is brought to approximately 80° C. (slight boiling of the ethanol) and the mixture is stirred at 600 rpm. The mixture is held at 80° C. for 2 hours. Gradually the solids (Na₂S and sulfur) disappear and the mixture changes from yellow to orange, then to brown. At the end of reaction the mixture is homogeneous at 80° C.; this gives approximately 58 g of anhydrous Na₂S₄ (0.33 mol) in 600 ml of ethanol.

3.2) Preparation of 7:

114 g of chloropropyldimethylethoxysilane 5 with a molar purity of 96.6% (i.e., 0.61 mol) are introduced via a dip tube, using a pump, into the anhydrous Na₂S₄ in 600 ml of ethanol, prepared above, which is maintained in its preparation reactor at 80° C. (slight boiling of the ethanol) and stirred at 600 rpm. A sodium chloride precipitate appears. When the introduction of chloropropyldimethylethoxysilane 5 is at an end, the mixture is held at 80° C. for 2 hours. Subsequently the mixture is cooled to room temperature, withdrawn and then filtered to remove the suspended solids, including the sodium chloride. The filtercake is washed with ethanol in order to extract as much as possible of the organic products from it. The filtrate is reintroduced into the reactor in order to be distilled therein under reduced pressure (approximately 20×10² Pa) for the purpose of removing the ethanol and any light products. 114 g of residue are recovered, which corresponds to bis(monoethoxydimethylsilylpropyl) tetrasulfide, assayed at a purity of 97% (molar).

This gives a mass yield of bis(monoethoxydimethylsilylpropyl) tetrasulfide of 87%.

Checking by ¹H NMR, by ²⁹Si NMR and ¹³C NMR makes it possible to verify that the structure obtained is in accordance with the formula (III) given in the description.

The average number of S atoms per molecule of formula (III) is 3.9±0.1 (x=3.9±0.1).

EXAMPLES 2 TO 8

Step b) of example 1 is carried out again with the exception that the sites at which the alcohol is injected into the column, and/or the EtOH/silane molar ratio, and/or the reflux rate are modified. The results obtained are collated in Table 1 below, where DC and RT represent respectively the degree of conversion of chloropropyldimethylchlorosilane and the selectivity for chloropropyldimethylethoxysilane:

TABLE 1 Plate of Plate of EtOH silane EtOH/silane Reflux Example injection injection molar ratio DC RT rate 1 12 13 1.2 20 88 0.5 2 12 13 3 70 93 0.5 3 12 13 6 68 91 0.5 4 3 13 1.2 35 89 0.5 5 3 13 3 92 91 0.5 6 3 13 6 91 91 0.5 7 3 13 10 89 90 0.5 8 3 13 3 93.5 86 1

From table 1 it emerges that it is preferable to have an EtOH/silane molar ratio of more than 3 in order to ensure that DC and RT values of more than 90 are obtained.

It is also apparent that it is preferable to inject EtOH onto plate 3 rather than onto plate 12. In this latter case the reaction volume is inadequate.

Another parameter is the reflux rate. This reflux rate controls the temperature level in the column but in particular in the amount of HCl (dissolved in the ethanol). And it is this acid which activates parasitic chemical reactions: example 8 is carried out with a reflux twice as great as in example 5, and, with all other things being equal, leads to a slight increase in the yield but to the detriment of the selectivity (86% and 91% respectively for examples 8 and 5).

EXAMPLE 9

A continuous reaction is carried out in the same column as for the preceding examples but without inert solvent. On this occasion the boiler (2) is charged with ethanol (1200 ml). The column (1) is charged by bringing the ethanol in the boiler (2) to boiling and by working at total reflux. When the steady-state regime has been attained the reflux is regulated and the 3-chloropropyldimethylchlorosilane is injected onto plate 13.

The ethanol flow rate (gas phase) is controlled by keeping the level in the boiler constant. The ethanol flow rate is 500 g/h and the chloropropyldimethylchlorosilane flow rate is 150 g/h, giving an EtOH:silane molar ratio of 12. The yield of the reaction is 100% irrespective of the reflux rate. Conversely the selectivity is a function of this reflux rate: from 50% for a reflux of 750 g/h to more than 85% for a zero reflux. It should be noted that in the column used, even at zero reflex, a fraction of the ethanol is condensed directly in the column. This can be avoided by introducing chloropropyldimethylchlorosilane preheated to 80° C. beforehand in order to prevent the cooling of the ethanol and its condensation.

EXAMPLE 10

Same experiment as example 3 with introduction of the chloropropyldimethylchlorosilane at plate 7. The results are identical to the preceding example: DC 100% and RT>85%. 

1. A process for preparing bis(monoorganoxysilylpropyl) polysulfides of formula (I):

in which: x, the average number of sulfur atoms per molecule, is an integral or fractional number ranging from 1.5±0.1 to 5±0.1; the symbols R¹, which are identical or different, each represent a monovalent hydrocarbon group selected from a linear or branched alkyl radical having 1 to 15 carbon atoms and a linear or branched alkoxyalkyl radical having 2 to 8 carbon atoms; the symbols R² and R³, which are identical or different, each represent a monovalent hydrocarbon group selected from a linear or branched alkyl radical having 1 to 6 carbon atoms and a phenyl radical; said process being performed by carrying out the following steps: a) reacting a diorganohalosilane of formula (V) with an allyl compound of formula (VI) to form a diorganohalosilylpropyl compound of formula (VII)

wherein: the symbol Hal represents a halogen atom selected from chlorine, bromine and iodine, the symbols R² and R³ are as defined above, and A represents a removable group selected from the group consisting of a halogen atom selected from chlorine, bromine and iodine, a radical para-R⁰—C₆H₄—SO₂—O—, wherein R⁰ is a linear or branched C1-C4 alkyl radical, a radical R⁰—SO₂—O—, wherein R⁰ is as defined above, or a radical R⁰—CO—O— wherein R⁰ is as defined above, said reaction occurring at a temperature ranging from −10° C. to 200° C. in the presence of an initiator comprising either: a catalytic activator consisting of: (i) at least one catalyst comprising at least one transition metal selected from the group consisting of Co, Ru, Rh, Pd, Ir and Pt; and optionally (2i) at least one hydrosilylation reaction promoter, or a photochemical activator, and, optionally, isolating the diorganohalosilylpropyl derivative of formula (VII) formed; b) preparing an organodialkylalkoxysilane of formula (IX): R¹O—(R₂R₃)Si—(CH₂)₃-A  (IX) by reacting a diorganohalosilylpropyl derivative of formula (VII) with an alcohol of formula (VIII)

R¹—OH  (VIII) by continuously contacting the alcohol of formula (VIII) in countercurrent with the silane of formula (VII) to produce a reaction mixture comprising the organodialkylalkoxysilane of formula (IX), wherein a product H-Hal is formed and is removed, and optionally isolating the organodialkylalkoxysilane of formula (IX); and c) forming the bis(monoorganoxysilylpropyl) polysulfide of formula (I) by reacting the monoorganoxydiorganosilylpropyl derivative of formula (IX) R¹O—(R₂R₃)Si—(CH₂)₃-A  (IX) with a metal polysulfide of formula (X) M₂S_(x)  (X) wherein: the symbols R¹, R², R³, A and x are as defined above and the symbol M represents an alkali metal, said reaction being carried out: by reacting, at a temperature ranging from 20° C. to 120° C., either the reaction mixture obtained at the end of step b), or the isolated monoorganoxydiorganosilylpropyl derivative of formula (IX) from step b), with the metal polysulfide of formula (X) in the anhydrous state, using 0.5±15 mol % of metal polysulfide of formula (X) per mole of the reactant of formula (IX), optionally in the presence of an inert organic solvent, and by isolating the bis(monoorganoxysilylpropyl) polysulfide of formula (I) that is formed.
 2. The process according to claim 1, wherein step (a) is carried out in the presence of a catalytic activator which comprises, as the catalyst(s) (i), at least one of the following metal species: (i-1) at least one finely divided elemental transition metal; and/or (i-2) a colloid of at least one transition metal; and/or (i-3) an oxide of at least one transition metal; and/or (i-4) a salt of at least one transition metal and a mineral or carboxylic acid; and/or (i-5) a complex of at least one transition metal with organic ligand(s) possessing one or more heteroatoms and/or organosilicon ligands; and/or (i-6) a salt derived from at least one transition metal and a mineral or carboxylic acid in which the transition metal is complexed with organic ligand(s) possessing one or more heteroatoms and/or organosilicon ligands; and/or (i-7) a metal species selected from an elemental transition metal, oxide, salt, complex and complexed salt wherein the transition metal is combined with at least one other metal selected from the class of the elements of groups Ib, 2b, 3a, 3b, 4a, 4b, 5a, 5b, 6b, 7b and 8 with the exception of Co, Ru, Rh, Pd, Ir and Pt, of the Periodic Table, said other metal being in its elemental form or in a molecular form.
 3. The process according to claim 2, wherein the transition metal in the catalyst (or catalysts) is selected from Ir and Pt.
 4. The process according to claim 3, wherein the transition metal in the catalyst (or catalysts) is Ir.
 5. The process according to claim 4, wherein step (a) is carried out in the presence of a catalytic activator comprising, as the catalyst (or catalysts) (i), at least one metal species of type (i-5) belonging to the iridium complexes of formula: [Ir(R⁴)Hal]₂  (XI) wherein: the symbol R⁴ represents a conjugated or non-conjugated, linear or cyclic (mono- or polycyclic) polyene ligand having 4 to 22 carbon atoms and from 2 to 4 ethylenic double bonds; and the symbol Hal represents a halogen atom selected from chlorine, bromine and iodine atoms.
 6. The process according to claim 1, wherein the anhydrous metal polysulfides of formula (X) used in step c) are prepared from an alkali metal sulfide M₂S in the form of a hydrated sulfide, according to a procedure comprising the steps of: (1) dehydrating the alkali metal sulfide hydrate to remove the water of crystallization while retaining the alkali metal sulfide in the solid state throughout the dehydration phase; and (2) reacting the dehydrated alkali metal sulfide with elemental sulfur, where the alkali metal sulfide is reacted with elemental sulfur with a ratio of one mole of dehydrated alkali metal sulfide to n(x−1) moles of elemental sulfur, wherein the reaction is carried out at a temperature ranging from 20° C. to 120° C., optionally under pressure and optionally in the presence of an anhydrous organic solvent, the aforementioned factor n has a value within the range from 0.8 to 1.2 and the symbol x is an integral or fractional number ranging from 1.5±0.1 to 5±0.1.
 7. The process according to claim 6, wherein R¹ is an ethyl group, R² and R³ are methyl groups, and A and Hal are each a chlorine atom in the compounds corresponding to formulae (I), (V), (VI), (VII), (VIII) and (IX). 